Hydrotreating catalyst containing phosphorus and boron

ABSTRACT

A catalyst having at least one Group VIB metal component, at least one Group VIII metal component, a phosphorus component, and a boron-containing carrier component. The amount of the phosphorus component is at least 1 wt %, expressed as an oxide (P2O5) and based on the total weight of the catalyst, and the amount of boron content is in the range of about 1 to about 13 wt %, expressed as an oxide (B2O3) and based on the total weight of the catalyst. In one embodiment of the invention, the boron-containing carrier component is a product of a co-extrusion of at least a carrier and a boron source. A method for producing the catalyst and its use for hydrotreating a hydrocarbon feed are also described.

REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No.13/265,728, filed Oct. 21, 2011, which application is the National Stageof International Patent Appl. No. PCT/EP2010/002458 filed on Apr. 21,2010, which in turn claims the benefit of U.S. Provisional Patent Appl.No. 61/171,253, filed on Apr. 21, 2009, the disclosures of which areincorporated herein by reference.

TECHNICAL FIELD

The present invention is in the field of catalysts useful forhydrotreating hydrocarbon feedstocks in refining processes.

THE INVENTION

In general, hydrotreating catalysts are composed of a carrier havingdeposited thereon a Group VIB (of the Periodic Table) metal componentand a Group VIII (of the Periodic Table) metal component. The mostcommonly employed Group VIB metals are molybdenum and tungsten, whilecobalt and nickel are the conventional Group VIII metals. Phosphorus mayalso be present in the catalyst. The prior art processes for preparingthese catalysts are characterized in that a carrier material iscomposited with hydrogenation metal components, for example byimpregnation, after which the composite is calcined to convert the metalcomponents into their oxides. Before being used in hydrotreating, thecatalysts are generally presulfided to convert the hydrogenation metalsinto their sulfides. Processes for activating and regenerating suchcatalysts are also known.

However, unexpectedly, highly effective catalysts containing a uniquecombination of both phosphorus and boron have now been discovered. Inparticular, it has been discovered that surprisingly significantimprovement in catalytic activity can be achieved using particular,relatively elevated amounts of both boron and phosphorus components inthe catalyst.

Thus, in one embodiment of the invention there is provided a catalystcomprising at least one Group VIB metal component, at least one GroupVIII metal component, a phosphorus component, and a boron-containingcarrier component, wherein the amount of the phosphorus component is atleast 1 wt %, expressed as an oxide (P₂O₅) and based on the total weightof the catalyst, and the amount of the boron component is in the rangeof about 1 to about 13 wt %, expressed as an oxide (B₂O₃) and based onthe total weight of the catalyst. In a particularly preferred embodimentof the invention, the boron-containing carrier is formed by co-extrusionof a boron source with the carrier.

In another embodiment of the invention, provided is a method ofproducing a catalyst. The method comprises co-extruding a boron sourcewith a carrier to form a boron-containing carrier extrudate, drying andcalcining the extrudate, and impregnating the calcined extrudate with asolution comprised of a phosphorus source, at least one Group VIB metalsource and/or at least one Group VIII metal source. Co-extrusion of theboron source has been found to be particularly and surprisinglyadvantageous when compared to, e.g., preparing the support viaimpregnation of the boron source. One feature co-extrusion is that itenable use of higher boron concentrations in the carrier and, therefore,the final catalyst. Co-extrusion with the carrier also permits a singlecalcination of the combined support, rather than multiple calcinationsteps as in typical impregnation procedures. In the process, the amountof the boron source and the amount of the phosphorus source issufficient so as to form a catalyst composition at least having a boroncontent in the range of about 1 wt % to about 13 wt %, expressed as anoxide (B₂O₃) and based on the total weight of the catalyst, and aphosphorus content of at least about 1 wt %, expressed as an oxide(P₂O₅) and based on the total weight of the catalyst.

In another embodiment of the invention there is provided a catalystcomposition formed by the just above-described process. Anotherembodiment of the invention is a hydrotreating process carried outemploying the catalyst composition.

These and still other embodiments, advantages and features of thepresent invention shall become further apparent from the followingdetailed description, including the appended claims.

FURTHER DETAILED DESCRIPTION OF THE INVENTION

Unless otherwise indicated, weight percent (wt %) as used herein is theweight percent of the specified form of the substance, based upon thetotal weight of the product for which the specified substance or form ofsubstance is a constituent or component. It should further be understoodthat, when describing steps or components or elements as being preferredin some manner herein, they are preferred as of the initial date of thisdisclosure, and that such preference(s) could of course vary dependingupon a given circumstance or future development in the art. Moreover,“boron source” and “boron component” are used herein interchangeably andare synonymous with one another. Also, the term “boron-containingcarrier” is intended to refer to any carrier as specified herein whichhas been contacted with a boron source prior to drying and calcining,and preferably “contacted” in this context shall encompass mixing, andin particular, co-extrusion.

The Group VIB metal component in catalysts of the invention is selectedfrom the group consisting of molybdenum, tungsten, chromium and amixture of two or more of the foregoing, while molybdenum and/ortungsten is typically preferred, and molybdenum is typically morepreferred. The Group VIII metal component is selected from groupconsisting of iron, cobalt and nickel, while nickel and/or cobalt istypically preferred, and nickel is typically more preferred. Preferredmixtures of metals include a combination of (a) nickel and/or cobalt and(b) molybdenum and/or tungsten. When hydrodesulfurisation (sometimeshereafter referred to as “HDS”) activity of the catalyst is important, acombination of cobalt and molybdenum is advantageous and typicallypreferred. When hydrodenitrogenation (sometimes hereafter referred to as“HDN”) activity of the catalyst is important, a combination of nickeland either molybdenum or tungsten is advantageous and typicallypreferred.

The Group VIB metal component can be an oxide, an oxo acid, or anammonium salt of an oxo or polyoxo anion. The Group VIB metal compoundsare formally in the +6 oxidation state. Oxides and oxo acids arepreferred Group VIB metal compounds. Suitable Group VIB metal compoundsin the practice of this invention include chromium trioxide, chromicacid, ammonium chromate, ammonium dichromate, molybdenum trioxide,molybdic acid, ammonium molybdate, ammonium para-molybdate, tungstentrioxide, tungstic acid, ammonium tungsten oxide, ammonium metatungstatehydrate, ammonium para-tungstate, and the like. Preferred Group VIBmetal compounds include chromium trioxide, molybdenum trioxide, molybdicacid, tungstic acid and tungsten trioxide. Mixtures of any two or moreGroup VIB metal compounds can be used; a mixture of products will beobtained when compounds having different Group VIB metal are used. Theamount of Group VIB metal compound employed in the catalyst willtypically be in the range of about 18 to about 28 wt % (as trioxide),based on the total weight of the catalyst, but could be as low as, e.g.,16 wt %. In one embodiment of this invention, the amount of Group VIBmetal compound is in the range of about 19 to about 26 wt %, or about 22to about 26 wt % (as trioxide), based on the total weight of thecatalyst.

The Group VIII metal component is usually an oxide, hydroxide or salt,preferably a salt. Suitable Group VIII metal compounds include, but arenot limited to, cobalt oxide, cobalt hydroxide, cobalt nitrate, cobaltcarbonate, cobalt hydroxy-carbonate, cobalt acetate, cobalt citrate,nickel oxide, nickel hydroxide, nickel nitrate, nickel carbonate, nickelhydroxy-carbonate, nickel acetate, and nickel citrate. Preferred GroupVIII metal compounds include cobalt carbonate, cobalt hydroxy-carbonate,nickel hydroxy-carbonate and nickel carbonate. Mixtures of two or moreGroup VIII metal compounds can be used; when the Group VIII metals ofthe compounds in the mixture are different, a mixture of products willbe obtained. The amount of Group VIII metal compound employed in thecatalyst will typically be in the range of about 2 to about 8 wt % (asoxide), based on the total weight of the catalyst. In a preferredembodiment of this invention, the amount of Group VIII metal compound isin the range of about 3 to about 6 wt % (as oxide), based on the totalweight of the catalyst.

In the practice of this invention, the phosphorus component is acompound which is typically a water soluble, acidic phosphorus compound,particularly an oxygenated inorganic phosphorus-containing acid.Examples of suitable phosphorus compounds include metaphosphoric acid,pyrophosphoric acid, phosphorous acid, orthophosphoric acid,triphosphoric acid, tetraphosphoric acid, and precursors of acids ofphosphorus, such as ammonium hydrogen phosphates (mono-ammoniumdi-hydrogen phosphate, di-ammonium mono-hydrogen phosphate, tri-ammoniumphosphate). Mixtures of two or more phosphorus compounds can be used.The phosphorus compound may be used in liquid or solid form. A preferredphosphorus compound is orthophosphoric acid (H₃PO₄) or an ammoniumhydrogen phosphate, preferably in aqueous solution. The amount ofphosphorus compound employed in the catalyst will be sufficient toprovide at least about 1 wt % (as oxide P₂O₅), based on the total weightof the catalyst, or in another aspect of the invention, at least about 2wt % (as oxide P₂O₅), based on the total weight of the catalyst. Inanother aspect, the amount of phosphorus compound employed will besufficient to provide phosphorus in the range of about 4 to about 10 wt% (as oxide P₂O₅), based on the total weight of the catalyst. In anotheraspect of this invention, the amount of phosphorus compound employed issufficient to provide phosphorus in the range of about 4 to about 7 wt %(as oxide P₂O₅), based on the total weight of the catalyst.

The boron component will typically be meta-boric acid (HBO₂),ortho-boric acid (H₃BO₃), ammonium borate tetra-hydrate[(NH₄)₂B₄O₇.4H₂O], sodium tetra borate, ammonium borate, ammonium tetraborate (NH₄)₂B4O7, boric oxide (B₂O₃), various mono-, di- and tri-alkylamine borates (e.g., triethanol amine borate), ammonium tetra phenylborate, or the like. Suitable non-limiting examples of the boroncomponent include ortho-boric acid (H₃BO₃) and ammonium tetra boratetetra-hydrate [(NH₄)₂B₄O₇.4H₂O] and mixtures of two or more of theforegoing. The amount of the boron component in the catalyst willtypically be in the range of about 1 to about 13 wt %, expressed as anoxide (B₂O₃) and based on the total weight of the catalyst. In apreferred embodiment of this invention, the amount of boron component isin the range of about 2 wt % to about 8 wt %, expressed as an oxide(B₂O₃) and based on the total weight of the catalyst. In another aspectof the invention, the amount of boron component is in the range of about4 wt % to about 6 wt %, expressed as an oxide (B₂O₃) and based on thetotal weight of the catalyst.

The catalyst carrier may comprise the conventional oxides, e.g.,alumina, silica, silica-alumina, alumina with silica-alumina dispersedtherein, silica-coated alumina, alumina-coated silica, magnesia,zirconia, and titania, as well as mixtures of these oxides. As a rule,preference is given to the carrier being of alumina, silica-alumina,alumina with silica-alumina dispersed therein, alumina-coated silica orsilica-coated alumina. Special preference is given to alumina andalumina containing up to 10 wt % of silica. A carrier containing atransition alumina, for example an eta, theta, or gamma alumina ispreferred within this group, wherein a gamma-alumina carrier is mostespecially preferred. The precursor of the catalyst carrier co-extrudedwith the boron source of this invention prior to calcination is, forexample, boehmite, pseudo-boehmite or the like, and can be in the formof a wet cake or dried (e.g., spray-dried) material.

As noted earlier, it is preferred that the boron component isco-extruded with the carrier component, as it is believed, without beingbound to theory, that co-extrusion facilitates use of the higherconcentration of boron component employed in the highly active catalystof this invention. It is further believed, without being bound totheory, that the moment of boron component addition to the carrier forco-extrusion can affect the physical properties of the carrier. It istherefore typically preferred, although not always required orpreferred, that addition of the boron component is carried out at theinitiation of kneading. The desired properties of the final product maydictate that one add the boron component earlier or later in thekneading process.

The catalyst's pore volume (measured via mercury penetration, contactangle 140°, surface tension of 480 dyn/cm) is not critical to theprocess according to the invention and will generally be in the range of0.2 to 2 ml/g, preferably 0.3-1 ml/g. The specific catalyst surface areais not critical to the process according to the invention either andwill generally be in the range of 50 to 400 m²/g (measured using the BETmethod). Preferably, the catalyst will have a median pore diameter inthe range of 7-15 nm, as determined by mercury porosimetry, and at least60% of the total pore volume will be in the range of +−0.2 nm from themedian pore diameter.

The catalyst is employed in the conventional manner in the form of, forexample, spheres or extrudates. Examples of suitable types of extrudateshave been disclosed in the literature (see, int al., U.S. Pat. No.4,028,227). Highly suitable for use are cylindrical particles (which maybe hollow or not) as well as symmetrical and asymmetrical polylobedparticles (2, 3 or 4 lobes).

In forming the catalyst of this invention, the amount of the boronsource and the amount of the phosphorus source should be sufficient soas to form a catalyst composition at least having a boron content in therange of about 1 wt % to about 13 wt %, expressed as an oxide (B₂O₃) andbased on the total weight of the catalyst, and a phosphorus content ofat least about 1 wt %, expressed as an oxide (P₂O₅) and based on thetotal weight of the catalyst.

Formation of the catalyst will normally involve at least co-extruding aboron source with a carrier to form a boron-containing carrierextrudate, drying and calcining the extrudate, and impregnating thecalcined extrudate with a solution comprised of a phosphorus source, atleast one Group VIB metal source and/or at least one Group VIII metalsource. Other additives to the solution optionally may be included, suchas organic additives such as (i) an organic compound selected from thegroup consisting of compounds comprising at least two oxygen atoms and2-10 carbon atoms and the compounds built up from these compounds, or(ii) an organic compound comprising at least one covalently bondednitrogen atom and at least one carbonyl moiety, or both (i) and (ii).The organic compound under (i) above preferably is selected from thegroup of compounds comprising at least two oxygen-containing moieties,such as a carboxyl, carbonyl or hydroxyl moiety, and 2-10 carbon atoms,and the compounds built up from these compounds. The latter may be,e.g., the ether, ester, acetal, acid chloride, acid amide, oligomer orpolymer of this organic compound. Examples of suitable organic compoundsinclude citric acid, tartaric acid, oxalic acid, malonic acid, malicacid, butanediol, pyruvic aldehyde, glycol aldehyde, and acetaldol.Organic compounds selected from the group of compounds comprising atleast two hydroxyl groups and 2-10 carbon atoms per molecule and thecompounds built up from these compounds are even more preferred. Theseinclude, e.g., tartaric acid, or aliphatic alcohols such as ethyleneglycol, propylene glycol, glycerin, trimethylol ethane, trimethylolpropane, etc. Compounds built up from these organic compounds includeoligo- and polymers, e.g., diethylene glycol, dipropylene glycol,trimethylene glycol, triethylene glycol, tributylene glycol,tetraethylene glycol, tetrapentylene glycol. This range can beextrapolated to include, e.g., polyethers like polyethylene glycol. Forthis last compound, polyethylene glycol with a molecular weight between200 and 8,000 is preferred. Other compounds built up from these organiccompounds are, e.g., ethers such as ethylene glycol monobutyl ether,diethylene glycol monomethyl ether, diethylene glycol monoethyl ether,diethylene glycol monopropyl ether, and diethylene glycol monobutylether. Preferred organic compounds are, int. al., ethylene glycol,diethylene glycol, polyethylene glycol, or mixtures thereof. Anothergroup of organic compounds comprising at least two hydroxyl groups and2-10 carbon atoms per molecule is formed by, e.g., monosaccharides suchas glucose and fructose. Compounds built up from these organic compoundsinclude oligo- and polymers, e.g., disaccharides such as lactose,maltose, and saccharose and polysaccharides.

The organic compound under (ii) preferably comprises at least twocarbonyl moieties. It is preferred that at least one carbonyl moiety ispresent in a carboxyl group. It is furthermore preferred that at leastone nitrogen atom is covalently bonded to at least two carbon atoms. Apreferred organic compound satisfies formula (I) or (II)

(R1R2)N—R3-N(R1′R2′)  (I)

N(R1R2R1′)  (II)

wherein R1, R2, R1′ and R2′ are independently selected from alkyl,alkenyl, and allyl, with up to 10 carbon atoms optionally substitutedwith one or more groups selected from carbonyl, carboxyl, ester, ether,amino, or amido. R3 is an alkylene group with up to 10 carbon atomswhich may be interrupted by —O— or —NR4-. R4 is selected from the samegroup as indicated above for R1. The R3 alkylene group may besubstituted with one or more groups selected from carbonyl, carboxyl,ester, ether, amino, or amido. As has been set out above, it isessential that the organic compound of formula (I) or (II) comprises atleast one carbonyl moiety. Preferably, at least two of R1, R2, R1′ andR2′ (formula (I)) and at least two of R1, R2 and R1′ (formula (II)) havethe formula —R5-COOX, wherein R5 is an alkylene group having 1-4 carbonatoms, and X is hydrogen or another cation, such as an ammonium, sodium,potassium and/or lithium cation. If X is a multivalent cation, one X canadhere to two or more —R5-COO groups. Typical examples of a compound offormula (I) are ethylene diamine(tetra)acetic acid (EDTA),hydroxyethylene diamine triacetic acid, and diethylene triaminepentaacetic acid. A typical example of a compound of formula (II) isnitrilotriacetic acid (NTA).

The co-extrusion is carried out by adding the boron component to thealumina precursor component during the kneading step. The moment ofaddition is not fixed. The boron component is added as a solid/solution.During the kneading step, the mix is heated to a desired temperature toremove any excess of solvent/water if needed. Kneading is finished whenthe desired moisture content (as determined by Loss on Ignition at atemperature in the range of 500−600° C.) is reached. Next, the mix isshaped to extrudates by using a suitable shaping technique. Thistechnique can be extrusion, palletizing or pressing.

The extrudate so formed is then dried at a temperature in the range of80°-200° C. to remove a substantial amount of solvent/water and thencalcined under air or inert conditions with or without steam at atemperature normally in the range of 400°-900° C., resulting in the caseof alumina, in a carrier containing a transition alumina e.g., a gamma,theta or eta-alumina, although a temperature outside of the latter rangeis possible, depending upon the support material employed. Thecalcination can be in a static or rotating mode. As will now be known bythose of skill in the art, the drying times and calcining times employedcan vary significantly depending upon various factors, including withoutlimitation the temperature ramp rate, if any, and the types and amountsof materials present, but in all cases should be sufficient to removevolatiles to the extent desired, or to permit desired reactions tosufficiently take place. Typical drying time will be, e.g., at least 30minutes at the maximum drying temperature, and typical calcining timewill be, e.g., at least 30 minutes at the maximum calcining temperature.

The calcined extrudate is then impregnated with a solution comprisingthe phosphorous source, a Group VIB metal source and/or a Group VIIImetal source. Impregnation is carried out by pore volume impregnationwith a impregnation solution comprising the selected additives in anappropriate solvent. The solvent used in preparing the additiveimpregnation solution is generally water, although other components suchas methanol, ethanol and other alcohols may also be suitable.Impregnation can be carried out at room temperature or at elevatedtemperatures. Instead of impregnating techniques, dipping methods,spraying methods, etc can be used. After impregnation, an optionaldrying step at a temperature in the range of 25-220° C. is carried out.In another embodiment of the invention, when no organic additive hasbeen incorporated to produce the final catalyst, the impregnatedcalcined extrudate can optionally be again calcined at a temperature inthe range of about 250 to about 700° C. until a desired Loss on Ignitionis reached.

Optionally, catalysts of the invention may be subjected to a sulfidationstep (treatment) to convert the metal components to their sulfides. Inthe context of the present specification, the phrases “sulfiding step”and “sulfidation step” are meant to include any process step in which asulfur-containing compound is added to the catalyst composition and inwhich at least a portion of the hydrogenation metal components presentin the catalyst is converted into the sulfidic form, either directly orafter an activation treatment with hydrogen. Suitable sulfidationprocesses are known in the art. The sulfidation step can take place exsitu to the reactor in which the catalyst is to be used in hydrotreatinghydrocarbon feeds, in situ, or in a combination of ex situ and in situto the reactor.

Ex situ sulfidation processes take place outside the reactor in whichthe catalyst is to be used in hydrotreating hydrocarbon feeds. In such aprocess, the catalyst is contacted with a sulfur compound, e.g., apolysulfide or elemental sulfur, outside the reactor and, if necessary,dried. In a second step, the material is treated with hydrogen gas atelevated temperature in the reactor, optionally in the presence of afeed, to activate the catalyst, i.e., to bring the catalyst into thesulfided state.

In situ sulfidation processes take place in the reactor in which thecatalyst is to be used in hydrotreating hydrocarbon feeds. Here, thecatalyst is contacted in the reactor at elevated temperature with ahydrogen gas stream mixed with a sulphiding agent, such as hydrogensulfide or a compound which under the prevailing conditions isdecomposable into hydrogen sulphide. It is also possible to use ahydrogen gas stream combined with a hydrocarbon feed comprising a sulfurcompound which under the prevailing conditions is decomposable intohydrogen sulfide. In the latter case, it is possible to sulfide thecatalyst by contacting it with a hydrocarbon feed comprising an addedsulfiding agent (spiked hydrocarbon feed), and it is also possible touse a sulfur-containing hydrocarbon feed without any added sulfidingagent, since the sulfur components present in the feed will be convertedinto hydrogen sulfide in the presence of the catalyst. Combinations ofthe various sulfiding techniques may also be applied. The use of aspiked hydrocarbon feed may be preferred.

The catalyst compositions of this invention are those produced by theabove-described process, whether or not the process included an optionalsulfiding step.

The formed catalyst product of this invention is suitable for use inhydrotreating, hydrodenitrogenation and/or hydrodesulfurization (alsocollectively referred to herein as “hydrotreating”) of hydrocarbon feedstocks when contacted by the catalyst under hydrotreating conditions.Such hydrotreating conditions are temperatures in the range of 250°-450°C., pressure in the range of 5-250 bar, liquid space velocities in therange of 0.1-10 liter/hour and hydrogen/oil ratios in the range of50-2000 N1/1. Examples of suitable hydrocarbon feeds to be so treatedvary widely, and include middle distillates, kero, naphtha, vacuum gasoils, heavy gas oils, and the like.

The following describes experimental preparation of the support and thecatalyst, as well as use of the catalyst in hydrotreating a hydrocarbonfeedstock to illustrate activity of the catalysts so formed. Thisinformation is illustrative only, and is not intend to limit theinvention in any way.

EXAMPLES Activity Test

The activity test was carried out in a micro flow reactor. Light Gas Oil(LGO) spiked with dimethyl disulfide (DMDS) (total S content of 3.6 wt%) was used for presulphiding, Heavy Gas Oil (HGO), having a S contentof 1.6 wt. % and N content of 1050 ppm, Vacuum Gas Oil (VGO), having a Scontent of 1.8 wt. % and N content of 1152 ppm and Light Gas Oil (LGO),having a S content of 1.2 wt. % and a N content of 94 ppm, were used fortesting. Detailed information about feed and test condition is given inTables 1-5.

The relative weight activities for the various catalysts were determinedas follows. For each catalyst the reaction constant k wt was calculatedfrom the following formula:

k wt=WHSV*1/(n−1)×(1/Sn ⁻¹×1/S ₀ ^(n−1))

in which the S stands for percentage of sulfur in the product and S₀ forthe percentage of sulfur in the feed, and n stands for the reactionorder of the hydrodesulfurisation reaction. For HC-PT and FCC-PT mode an of 1.75 was used. For ULSD a n of 1.2 was used For nitrogen the k wtwas calculated from the following formula:

k wt=ln(N ₀ /N)*WHSV

in which the N stands for the nitrogen content in the product and No forthe nitrogen content in the feed.

In the tables, S=sulfur, N=nitrogen, ToS=time on stream, LHSV=liquidhourly space velocity, IBP=initial boiling point, FBP=final boilingpoint.

TABLE 1 Feed properties IBP FBP Feed wt % S ppm N Density (g/ml) (° C.)(° C.) HGO 1.578 1050 0.9443 (@ 15.5 C) 139 482 VGO 1.763 1152 0.9221 (@15.5 C) 265 600 LGO 1.167 94 0.8366 (@ 15.5 C) 114 420

Presulfiding/Testing Conditions

TABLE 2 Test conditions HC-PT test, Feed HGO. Presulphiding TestingTemperature (° C.) 320 345 H2 pressure (bar) 45 100 LHSV 3 2.75 H2/oil300 1000 Time (hours) 27.5 * Feed LGO spiked with DMDS (total S contentof 3.6 wt %) was used for presulphiding. * Time on stream is reported inthe text of the examples.

TABLE 3 Test conditions HC-PT test, Feed VGO. Presulphiding TestingTemperature (° C.) 340 382 H2 pressure (bar) 30 120 LHSV 3 1.75 H2/oil300 1000 Time (hours) 27.5 * Feed LGO spiked with DMDS (total S contentof 3.6 wt %) was used for presulphiding. * Time on stream is reported inthe text of the examples.

TABLE 4 Test conditions FCC-PT test, Feed VGO. Presulphiding TestingTemperature (° C.) 320 360 H2 pressure (bar) 45 70 LHSV 3 1.2 H2/oil 300400 Time (hours) 16 * Feed LGO spiked with DMDS (total S content of 3.6wt %) was used for presulphiding. * Time on stream is reported in thetext of the examples.

TABLE 5 Test conditions ULSD test, Feed LGO. Presulphiding TestingTemperature (° C.) 320 340 H2 pressure (bar) 45 45 LHSV 3 2 H2/oil 300300 Time (hours) 27.1 * Feed LGO spiked with DMDS (total S content of3.6 wt %) was used for presulphiding. * Time on stream is reported inthe text of the examples.Support Preparation (0-18.75 wt % B₂O₃ in Support)

The support was prepared by mixing an alumina hydrate cake (watercontent about 80%) and boric acid (H₃BO₃) in a kneader to form anextrudable paste. (In some cases, the water content of the extrusion mixhad to be adjusted by evaporation or by adding additional water in orderto obtain a paste suitable for extrusion. A person skilled in the artknows how to adjust the water content in order to obtain an extrudablepaste.) The resulting mixture was extruded through a 1.3Q die plate,dried overnight at 120° C. and then calcined (optionally with steam) ata temperature in the range of 475-850° C. (See Table 6).

Support D3 was prepared from A1 and supports B₂, C3 and D4 were preparedfrom A6 by pore volume impregnation of the support A1 and A6,respectively, with a solution of ammonium tetra borate tetra hydrate((NH₄)₂B₄O_(7.4)H₂O) in water. The impregnated support was heated to atemperature of 120° C., kept at this temperature for 30 minutes andsubsequently calcined (optionally with steam) at a temperature in therange of 475-550° C. for 1 hour (See Table 6).

TABLE 6 Calcination temperature of the supports A-H Calcination SupportB₂O₃ (wt %) Temperature (° C.) A1 0 475 A2 0 600 A3 0 750 A4 0 840 A5 0720 A6 0 550 B1 1.88 700 B2 1.88 550 C1 3.75 700 C2 3.75 680 C3 3.75 550D1 7.5 760 D2 7.5 800 D3 7.5 475 D4 7.5 550 E1 9.8 650 E2 9.8 750 E3 9.8550 F1 11.25 810 F2 11.25 760 G1 15 850 H1 18.75 750

Preparation and Testing of Catalysts 1-44

All chemical compositions of the catalysts are calculated on basis ofthe amount of material used for the catalyst preparation.

Example 1 NiMoP Catalyst 1

The impregnation solution was prepared by mixing appropriate amounts ofwater, nickel carbonate [Ni(OH)_(x)(CO₃)_(Y)], molybdenum trioxide(MoO₃), and phosphoric acid (H₃PO₄). The mixture was sufficiently heatedand kept at temperature while stirred until a clear solution wasobtained. After the solution was cooled down, diethylene glycol (0.44mol/mol hydrogenation metals present in the catalyst) was added. Theinitial amount of water was chosen in a way that the total volume of thesolution after the addition of diethylene glycol was ca. 230% of thepore volume for the impregnation of the powdered support A4.

Support A4 was crushed, sieved and impregnated with the impregnationsolution to 230% pore volume saturation. The impregnated powder wasdried 10 hours at 80° C. and subsequently for 4 hours at 120° C. Thefinal MoO₃ content was 24 wt % (dry base) of the finished catalyst. Thefinal NiO content was 4 wt % (dry base) of the finished catalyst. Thefinal P₂O₅ content was 2 wt % (dry base) of the finished catalyst.

The catalyst was tested in HC-PT mode with HGO feed and reached aproduct S of 1026 ppm (k wt=21.05) and product N of 80 ppm (k wt=8.38)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 2 NiMoPB Catalyst 2

The powdered catalyst was prepared as described in Example 1, exceptthat support D1 was used and the final B₂O₃ content was 5.3 wt % (drybase) of the finished catalyst.

The catalyst was tested in HC-PT mode with HGO feed and reached aproduct S of 976 ppm (k wt=21.76) and product N of 29 ppm (k wt=11.54)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 3 NiMoPB Catalyst 3

The powdered catalyst was prepared as described in Example 1, exceptthat support G1 was used and that the final B₂O₃ content was 10.5 wt %(dry base) of the finished catalyst.

The catalyst was tested in HC-PT mode with HGO feed and reached aproduct S of 995 ppm (k wt=21.11) and product N of 23 ppm (k wt=12.24)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 4 NiMoP Catalyst 4

The powdered catalyst was prepared as described in Example 1, exceptthat the final P₂O₅ content was 4.5 wt % (dry base) of the finishedcatalyst.

The catalyst was tested in HC-PT mode with HGO feed and reached aproduct S of 902 ppm (k wt=23.10) and product N of 44 ppm (k wt=10.18)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 5 NiMoPB Catalyst 5

The powdered catalyst was prepared as described in Example 4, exceptthat support C1 was used and that the final B₂O₃ content was 2.5 wt %(dry base) of the finished catalyst.

The catalyst was tested in HC-PT mode with HGO feed and reached aproduct S of 910 ppm (k wt=21.90) and product N of 18 ppm (k wt=11.75)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 6 NiMoPB Catalyst 6

The powdered catalyst was prepared as described in Example 4, exceptthat support D1 was used and that the final B₂O₃ content was 5.1 wt %(dry base) of the finished catalyst.

The catalyst was tested in HC-PT mode with HGO feed and reached aproduct S of 926 ppm (k wt=22.31) and product N of 16 ppm (k wt=12.70)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 7 NiMoPB Catalyst 7

The powdered catalyst was prepared as described in Example 4, exceptthat support F1 was used and that the final B₂O₃ content was 7.6 wt %(dry base) of the finished catalyst.

The catalyst was tested in HC-PT mode with HGO feed and reached aproduct S of 1137 ppm (k wt=18.18) and product N of 16 ppm (k wt=12.70)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 8 NiMoPB Catalyst 8

The powdered catalyst was prepared as described in Example 4, exceptthat support G1 was used and that the final B₂O₃ content was 10.1 wt %(dry base) of the finished catalyst.

The catalyst was tested in HC-PT mode with HGO feed and reached aproduct S of 998 ppm (k wt=21.33) and product N of 23 ppm (k wt=12.43)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 9 NiMoP Catalyst 9

The powdered catalyst was prepared as described in Example 1, exceptthat the final P₂O₅ content was 7 wt % (dry base) of the finishedcatalyst.

The catalyst was tested in HC-PT mode with HGO feed and reached aproduct S of 1069 ppm (k wt=20.62) and product N of 34 ppm (k wt=10.57)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Catalyst 9 was also prepared as whole extrudates, following thepreparation procedure as described above, except that the total volumeof the impregnation solution after the addition of di ethylene glycolwas ca. 110% of the pore volume for the impregnation of extrudatessupport A4 and that the support was impregnated with the impregnationsolution to 110% pore volume saturation.

Extrudates of catalyst 9 were tested in HC-PT mode with HGO feed(product S of 653 ppm (k wt=28.74) and product N of 26 ppm (k wt=11.49)after 192 hours time on stream), in HC-PT mode with VGO feed (product Sof 583 ppm (k wt=19.84) and product N of 155 ppm (k wt=4.01) after 300hours time on stream) and in FCC-PT mode with VGO feed (product S of2022 ppm (k wt=4.72) and product N of 557 ppm (k wt=0.97) after 174hours time on stream).

Example 10 NiMoPB Catalyst 10

The powdered catalyst was prepared as described in Example 9, exceptthat support C1 was used and that the final B₂O₃ content was 2.4 wt %(dry base) of the finished catalyst.

The catalyst was tested in HC-PT mode with HGO feed and reached aproduct S of 964 ppm (k wt=20.97) and product N of 18 ppm (k wt=11.21)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Catalyst 10 was also prepared as whole extrudates, following thepreparation procedure as described above, except that the total volumeof the impregnation solution after the addition of di ethylene glycolwas ca. 110% of the pore volume for the impregnation of extrudatessupport C1 and that the support was impregnated with the impregnationsolution to 110% pore volume saturation.

Extrudates of catalyst 10 were tested in HC-PT mode with HGO feed(product S of 438 ppm (k wt=41.57) and product N of 12 ppm (k wt=14.26)after 192 hours time on stream) and in HC-PT mode with VGO feed (productS of 304 ppm (k wt=32.40) and product N of 92 ppm (k wt=4.65) after 300hours time on stream).

Example 11 NiMoPB Catalyst 11

The powdered catalyst was prepared as described in Example 9, exceptthat support D1 was used and that the final B₂O₃ content was 4.9 wt %(dry base) of the finished catalyst.

The catalyst was tested in HC-PT mode with HGO feed and reached aproduct S of 799 ppm (k wt=25.59) and product N of 11 ppm (k wt=14.17)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Catalyst 11 was also prepared as whole extrudates, following thepreparation procedure as described above, except that the total volumeof the impregnation solution after the addition of di ethylene glycolwas ca. 110% of the pore volume for the impregnation of extrudatessupport D1 and that the support was impregnated with the impregnationsolution to 110% pore volume saturation.

Extrudates of catalyst 11 were tested in HC-PT mode with HGO feed(product S of 349 ppm (k wt=47.72) and product N of 8 ppm (k wt=14.93)after 192 hours time on stream), in HC-PT mode with VGO feed (product Sof 300 ppm (k wt=31.84) and product N of 80 ppm (k wt=4.82) after 300hours time on stream) and in FCC-PT mode with VGO feed (product S of1805 ppm (k wt=5.46) and product N of 463 ppm (k wt=1.26) after 174hours time on stream).

Example 12 NiMoPB Catalyst 12

The powdered catalyst was prepared as described in Example 9, exceptthat support F1 was used and that the final B₂O₃ content was 7.3 wt %(dry base) of the finished catalyst.

The catalyst was tested in HC-PT mode with HGO feed and reached aproduct S of 1190 ppm (k wt=17.52) and product N of 21 ppm (k wt=11.35)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 13 NiMoPB Catalyst 13

The powdered catalyst was prepared as described in Example 9, exceptthat support G1 was used and that the final B₂O₃ content was 9.8 wt %(dry base) of the finished catalyst.

The catalyst was tested in HC-PT mode with HGO feed and reached aproduct S of 1043 ppm (k wt=20.21) and product N of 26 ppm (k wt=11.81)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 14 NiMoPB Catalyst 14

The powdered catalyst was prepared as described in Example 1, exceptthat support F1 was used and that the final P₂O₅ content was 9.5 wt %(dry base) and the final B₂O₃ content was 7.0 wt % (dry base) of thefinished catalyst.

The catalyst was tested in HC-PT mode with HGO feed and reached aproduct S of 1370 ppm (k wt=15.59) and product N of 30 ppm (k wt=11.48)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 15 NiMoPB Catalyst 15

The catalyst was prepared as whole extrudates as described in Example 9,except that support B₁ was used and that the final P₂O₅ content was 1.5wt % (dry base) and the final B₂O₃ content was 1.3 wt % (dry base) ofthe finished catalyst.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1220 ppm (k wt=8.06) and product N of 509 ppm (k wt=1.18)after 120 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 16 NiMoPB Catalyst 16

The powdered catalyst was prepared as described in Example 1, exceptthat support C2 was used and that the final MoO₃ content was 19 wt %(dry base), the final P₂O₅ content was 4 wt % (dry base) and the finalB₂O₃ content was 2.7 wt % (dry base) of the finished catalyst.

The catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1481 ppm (k wt=6.48) and product N of 545 ppm (k wt=1.03)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 17 NiMoPB Catalyst 17

The powdered catalyst was prepared as described in Example 16, exceptthat support F2 was used and that the final B₂O₃ content was 8.2 wt %(dry base) of the finished catalyst.

The catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1616 ppm (k wt=6.06) and product N of 521 ppm (k wt=1.11)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 18 NiMoP Catalyst 18

The catalyst was prepared as whole extrudates as described in Example 9,except that support A1 was used and that the final P₂O₅ content was 4.5wt % (dry base) of the finished catalyst.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1216 ppm (k wt=7.03) and product N of 455 ppm (k wt=1.16)after 120 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 19 NiMoPB Catalyst 19

The catalyst was prepared as whole extrudates as described in Example18, except that support B₁ was used and that the final B₂O₃ content was1.3 wt % (dry base) of the finished catalyst.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1230 ppm (k wt=7.85) and product N of 473 ppm (k wt=1.26)after 120 hours time on stream.

Example 20 NiMoPB Catalyst 20

The catalyst was prepared as whole extrudates as described in Example18, except that support B₂ was used and that the final B₂O₃ content was1.3 wt % (dry base) of the finished catalyst.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1115 ppm (k wt=7.33) and product N of 413 ppm (k wt=1.25)after 120 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 21 NiMoPB Catalyst 21

The catalyst was prepared as whole extrudates as described in Example 9,except that support C1 was used and that the final MoO3 content was 26wt % (dry base), the final NiO content was 5 wt % (dry base), the finalP₂O₅ content was 4.5 wt % (dry base) and the final B₂O₃ content was 2.4wt % (dry base) of the finished catalyst.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1407 ppm (k wt=6.63) and product N of 452 ppm (k wt=1.26)after 120 hours time on stream.

Example 22 NiMoPB Catalyst 22

The catalyst was prepared as whole extrudates as described in Example 9,except that support C1 was used and that the final MoO₃ content was 22wt % (dry base), the final NiO content was 3 wt % (dry base), the finalP₂O₅ content was 4.5 wt % (dry base) and the final B₂O₃ content was 2.6wt % (dry base) of the finished catalyst.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1664 ppm (k wt=6.14) and product N of 507 ppm (k wt=1.19)after 120 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 23 NiMoPB Catalyst 23

The catalyst was prepared as whole extrudates as described in Example22, except that support C1 was used and that the final NiO content was 5wt % (dry base) of the finished catalyst.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1282 ppm (k wt=7.87) and product N of 455 ppm (k wt=1.37)after 120 hours time on stream.

Example 24 NiMoPB Catalyst 24

The catalyst was prepared as whole extrudates as described in Example23, except that support C3 was used.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1231 ppm (k wt=7.08) and product N of 429 ppm (k wt=1.26)after 120 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 25 NiMoPB Catalyst 25

The catalyst was prepared as whole extrudates as described in Example18, except that support D3 was used and that the final B₂O₃ content was5.1 wt % (dry base) of the finished catalyst.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1488 ppm (k wt=5.62) and product N of 406 ppm (k wt=1.25)after 120 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 26 NiMoPB Catalyst 26

The catalyst was prepared as whole extrudates as described in Example25, except that support D2 was used.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1429 ppm (k wt=6.60) and product N of 419 ppm (k wt=1.37)after 120 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 27 NiMoPB Catalyst 27

The catalyst was prepared as whole extrudates as described in Example25, except that support H1 was used and that the final B₂O₃ content was12.7 wt % (dry base) of the finished catalyst.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1646 ppm (k wt=5.66) and product N of 436 ppm (k wt=1.28)after 120 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 28 NiMoPB Catalyst 28

The powdered catalyst was prepared as described in Example 1, exceptthat support D1 was used and that the final MoO₃ content was 19 wt %(dry base), the final P₂O₅ content was 6.5 wt % (dry base) and the finalB₂O₃ content was 5.3 wt % (dry base) of the finished catalyst.

The catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1473 ppm (k wt=6.09) and product N of 520 ppm (k wt=1.02)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 29 NiMoPB Catalyst 29

The powdered catalyst was prepared as described in Example 28, exceptthat support F2 was used and that the final B₂O₃ content was 7.9 wt %(dry base) of the finished catalyst

The catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1659 ppm (k wt=5.51) and product N of 486 ppm (k wt=0.94)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 30 NiMoP Catalyst 30

The catalyst was prepared as whole extrudates as described in Example 9,except that support A3 was used.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1597 ppm (k wt=5.50) and product N of 483 ppm (k wt=1.09)after 120 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 31 NiMoPB Catalyst 31

The catalyst was prepared as whole extrudates as described in Example 9,except that support C1 was used and that the final MoO₃ content was 22wt % (dry base), the final NiO content was 5 wt % (dry base), the finalP₂O₅ content was 7 wt % (dry base) and the final B₂O₃ content was 2.5 wt% (dry base) of the finished catalyst.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1206 ppm (k wt=7.81) and product N of 415 ppm (k wt=1.41)after 120 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 32 NiMoPB Catalyst 32

The catalyst was prepared as whole extrudates as described in Example31, except that support C3 was used.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1272 ppm (k wt=6.70) and product N of 416 ppm (k wt=1.27)after 120 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 33 NiMoPB Catalyst 33

The catalyst was prepared as whole extrudates as described in Example 9,except that support D2 was used and that the final B₂O₃ content was 4.9wt % (dry base) of the finished catalyst.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1313 ppm (k wt=6.56) and product N of 408 ppm (k wt=1.42)after 120 hours time on stream.

Example 34 NiMoPB Catalyst 34

The catalyst was prepared as whole extrudates as described in Example33, except that support D4 was used.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1275 ppm (k wt=6.44) and product N of 391 ppm (k wt=1.30)after 120 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 35 NiMoPB Catalyst 35

The catalyst was prepared as whole extrudates as described in Example34, except that support H1 was used and that the final B₂O₃ content was12.2 wt % (dry base) of the finished catalyst.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1592 ppm (k wt=5.62) and product N of 430 ppm (k wt=1.25)after 120 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 36 NiMoPB Catalyst 36

The powdered catalyst was prepared as described in Example 1, exceptthat support C2 was used and that the final MoO₃ content was 19 wt %(dry base), the final P₂O₅ content was 9 wt % (dry base) and the finalB₂O₃ content was 2.6 wt % (dry base) of the finished catalyst.

The catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1575 ppm (k wt=5.85) and product N of 533 ppm (k wt=1.01)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 37 NiMoPB Catalyst 37

The powdered catalyst was prepared as described in Example 36, exceptthat support D1 was used and that the final B₂O₃ content was 5.1 wt %(dry base) of the finished catalyst.

The catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1607 ppm (k wt=5.62) and product N of 559 ppm (k wt=0.93)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 38 NiMoPB Catalyst 38

The impregnation solution was prepared by mixing appropriate amounts ofwater, nickel carbonate [Ni(OH)_(x)(CO₃)_(Y)], molybdenum trioxide(MoO₃), and phosphoric acid (H₃PO₄). The mixture was sufficiently heatedand kept at temperature while stirred until a clear solution wasobtained. The initial amount of water was chosen in a way that the totalvolume of the solution was ca. 230% of the pore volume for theimpregnation of the powdered support C2.

Support C2 was crushed, sieved and impregnated with the impregnationsolution to 230% pore volume saturation. The impregnated powder wasdried for 10 hours at 80° C. and subsequently 4 hours at 120° C. Next,the dried catalyst was calcined for 1 hour at 480° C. The final MoO₃content was 19 wt % (dry base) of the finished catalyst. The final NiOcontent was 4 wt % (dry base) of the finished catalyst. The final P₂O₅content was 4 wt % (dry base) of the finished catalyst. The final B₂O₃content was 2.7 wt % (dry base) of the finished catalyst.

The catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1396 ppm (k wt=6.33) and product N of 448 ppm (k wt=1.20)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 39 NiMoP Catalyst 39

The powdered catalyst was prepared as described in Example 38, exceptthat support A5 was used and that the final P₂O₅ content was 6.5 wt %(dry base) of the finished catalyst.

The catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1191 ppm (k wt=8.18) and product N of 556 ppm (k wt=1.05)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 40 NiMoPB Catalyst 40

The powdered catalyst was prepared as described in Example 38, exceptthat support C2 was used and that the final P₂O₅ content was 6.5 wt %(dry base) of the finished catalyst.

The catalyst was tested in FCC-PT mode with VGO feed and reached aproduct S of 1576 ppm (k wt=5.52) and product N of 468 ppm (k wt=1.12)after 144 hours time on stream. Results are on basis of averagedduplicate measurements.

Example 41 CoMoP Catalyst 41

The extrudate catalyst was prepared as described in Example 9, exceptthat nickel carbonate was replaced by cobalt carbonate (CoCO₃) and thatsupport A2 was used. The final MoO₃ content was 24 wt % (dry base) ofthe finished catalyst. The final CoO content was 4.4 wt % (dry base) ofthe finished catalyst. The final P₂O₅ content was 2.1 wt % (dry base) ofthe finished catalyst.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in ULSD mode with LGO feed and reached aproduct S of 28.1 ppm (k wt=22.07) and product N of 1.15 ppm (kwt=10.18) after 216 hours time on stream. Results are on basis ofaveraged duplicate measurements.

Example 42 CoMoPB Catalyst 42

The extrudate catalyst was prepared as described in Example 41, exceptthat support E3 was used and that the final MoO₃ content was 25 wt %(dry base), the final CoO content was 6 wt % (dry base) and the finalB₂O₃ content was 6 wt % (dry base) of the finished catalyst.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in ULSD mode with LGO feed and reached aproduct S of 11.9 ppm (k wt=24.97) and product N of 0.3 ppm (k wt=12.18)after 216 hours time on stream.

Example 43 CoMoPB Catalyst 43

The extrudate catalyst was prepared as described in Example 41, exceptthat support E2 was used and that the final MoO₃ content was 25 wt %(dry base) and the final B₂O₃ content was 6.1 wt % (dry base) of thefinished catalyst.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in ULSD mode with LGO feed and reached aproduct S of 11.3 ppm (k wt=24.30) and product N of 0.3 ppm (k wt=11.71)after 216 hours time on stream.

Example 44 CoMoPB Catalyst 44

The extrudate catalyst was prepared as described in Example 41, exceptthat support E1 was used and that the final CoO content was 5 wt % (drybase), the final P₂O₅ content was 7.9 wt % (dry base) and the final B₂O₃content was 5.8 wt % (dry base) of the finished catalyst.

The catalyst was crushed and sieved, prior to the activity test. Thepowdered catalyst was tested in ULSD mode with LGO feed and reached aproduct S of 11.7 ppm (k wt=25.09) and product N of 0.3 ppm (k wt=12.19)after 216 hours time on stream.

Components referred to by chemical name or formula anywhere in thespecification or claims hereof, whether referred to in the singular orplural, are identified as they exist prior to coming into contact withanother substance referred to by chemical name or chemical type (e.g.,another component, a solvent, or etc.). It matters not what chemicalchanges, transformations and/or reactions, if any, take place in theresulting mixture or solution as such changes, transformations, and/orreactions are the natural result of bringing the specified componentstogether under the conditions called for pursuant to this disclosure.Thus the components are identified as ingredients to be brought togetherin connection with performing a desired operation or in forming adesired composition.

The invention may comprise, consist, or consist essentially of thematerials and/or procedures recited herein.

As used herein, the term “about” modifying the quantity of an ingredientin the compositions of the invention or employed in the methods of theinvention refers to variation in the numerical quantity that can occur,for example, through typical measuring and liquid handling proceduresused for making concentrates or use solutions in the real world; throughinadvertent error in these procedures; through differences in themanufacture, source, or purity of the ingredients employed to make thecompositions or carry out the methods; and the like. The term about alsoencompasses amounts that differ due to different equilibrium conditionsfor a composition resulting from a particular initial mixture. Whetheror not modified by the term “about”, the claims include equivalents tothe quantities.

Except as may be expressly otherwise indicated, the article “a” or “an”if and as used herein is not intended to limit, and should not beconstrued as limiting, the description or a claim to a single element towhich the article refers. Rather, the article “a” or “an” if and as usedherein is intended to cover one or more such elements, unless the textexpressly indicates otherwise.

Each and every patent or other publication or published documentreferred to in any portion of this specification is incorporated in totointo this disclosure by reference, as if fully set forth herein.

This invention is susceptible to considerable variation in its practice.Therefore the foregoing description is not intended to limit, and shouldnot be construed as limiting, the invention to the particularexemplifications presented hereinabove.

1. A catalyst comprising at least one Group VIB metal component, atleast one Group VIII metal component comprising nickel and/or cobalt, aphosphorus component, and a boron-containing carrier component, whereinthe amount of the phosphorus component is at least about 1 wt %,expressed as an oxide (P₂O₅) and based on the total weight of thecatalyst, and the boron content is in the range of about 1 to about 13wt %, expressed as an oxide (B₂O₃) and based on the total weight of thecatalyst; and wherein the formation of the catalyst involves at leastco-extruding a boron compound with a carrier to form a boron-containingcarrier extrudate, drying and calcining the extrudate, and impregnatingthe calcined extrudate with a solution comprised of a phosphorus source,at least one Group VIB metal source and/or at least one Group VIII metalsource.
 2. The catalyst according to claim 1 wherein the Group VIB metalcomponent comprises molybdenum.
 3. The catalyst according to claim 2wherein the Group VIII metal component comprises nickel.
 4. The catalystaccording to claim 2 wherein the Group VIII metal component comprisescobalt.
 5. The catalyst according to claim 1 wherein the Group VIIImetal component comprises nickel.
 6. The catalyst according claim 1wherein the carrier comprises alumina.
 7. The catalyst according toclaim 1 wherein the boron compound is selected from the group consistingof meta-boric acid, ortho-boric acid, ammonium borate tetra-hydrate,sodium tetra borate, ammonium borate, ammonium tetra borate, boricoxide, mono-, di- and tri-alkyl amine borate, ammonium tetra phenylborate, and a mixture of any two or more of the foregoing.
 8. Thecatalyst according to claim 1, further comprising an organic additive.9. The catalyst according to claim 8, wherein the organic additive isselected from the group consisting of (i) an organic compound selectedfrom the group consisting of (a) organic compounds comprising at leasttwo oxygen atoms and 2-10 carbon atoms, and (b) the ethers, esters,acetals, acid chlorides, acid amides, oligomers and polymers of theorganic compounds of (a), and/or (ii) an organic compound comprising atleast one covalently bonded nitrogen atom and at least one carbonylmoiety.
 10. A method of producing a catalyst, the method comprisingco-extruding a boron compound with a carrier to form a boron-containingcarrier extrudate, drying and calcining the extrudate, and impregnatingthe calcined extrudate with a solution comprised of a phosphorus source,at least one Group VIB metal source and/or at least one Group VIII metalsource comprising nickel and/or cobalt, the amount of the boron compoundand the amount of the phosphorus source being sufficient so as to form acatalyst composition at least having a boron content in the range ofabout 1 wt % to about 13 wt %, expressed as an oxide (B₂O₃) and based onthe total weight of the catalyst, and a phosphorus content of at leastabout 1 wt %, expressed as an oxide (P₂O₅) and based on the total weightof the catalyst.
 11. The method according to claim 10, furthercomprising calcining an impregnated calcined extrudate formed in theimpregnating step.
 12. The method according to claim 10, furthercomprising drying an impregnated calcined extrudate formed in theimpregnation step so as to form a dried impregnated calcined extrudateso as to form the catalyst.
 13. The method of claim 10, furthercomprising drying an impregnated calcined extrudate formed in theimpregnation step so as to form a dried impregnated calcined extrudate,and further calcining the dried impregnated calcined extrudate so as toform the catalyst.
 14. The method according to claim 10 wherein thesolution further comprises an organic additive.
 15. The method accordingto claim 14 wherein the organic additive is selected from the groupconsisting of (i) an organic compound selected from the group consistingof (a) organic compounds comprising at least two oxygen atoms and 2-10carbon atoms, and (b) the ethers, esters, acetals, acid chlorides, acidamides, oligomers and polymers of the organic compounds of (a), and/or(ii) an organic compound comprising at least one covalently bondednitrogen atom and at least one carbonyl moiety.
 16. A catalyst formed inaccordance with claim
 10. 17. A method which comprises contacting ahydrocarbon feed with a catalyst according to claim 1 underhydrotreating conditions so as to hydrotreat the hydrocarbon feed.
 18. Amethod which comprises contacting a hydrocarbon feed with a catalystaccording to claim 9 under hydrotreating conditions so as to hydrotreatthe hydrocarbon feed.
 19. The method according to claim 12 wherein thesolution further comprises an organic additive.
 20. The method accordingto claim 10 wherein the components consist of a boron compound, acarrier, and a solution comprised of a phosphorus source, at least oneGroup VIB metal source, at least one Group VIII metal source comprisingnickel and/or cobalt, and optionally an organic additive.
 21. The methodaccording to claim 20 wherein the organic additive is selected from thegroup consisting of (i) an organic compound selected from the groupconsisting of organic compounds comprising at least two oxygen atoms and2-10 carbon atoms, and the ethers, esters, acetals, acid chlorides, acidamides, oligomers or polymers thereof, and/or (ii) an organic compoundcomprising at least one covalently bonded nitrogen atom and at least onecarbonyl moiety.
 22. The catalyst according to claim 1 wherein thecomponents consist of at least one Group VIB metal component, at leastone Group VIII metal component comprising nickel and/or cobalt, aphosphorus component, a boron-containing carrier component, andoptionally an organic additive.
 23. The catalyst according to claim 22wherein the organic additive is selected from the group consisting of(i) an organic compound selected from the group consisting of (a)organic compounds comprising at least two oxygen atoms and 2-10 carbonatoms, and (b) the ethers, esters, acetals, acid chlorides, acid amides,oligomers and polymers of the organic compounds of (a), and/or (ii) anorganic compound comprising at least one covalently bonded nitrogen atomand at least one carbonyl moiety.
 24. The catalyst according to claim 9wherein the organic additive is selected from an organic compoundselected from the group consisting of organic compounds comprising atleast two oxygen atoms and 2-10 carbon atoms, and the ethers, esters,acetals, acid chlorides, acid amides, oligomers or polymers thereof.